JP2010525326A5 - - Google Patents
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- JP2010525326A5 JP2010525326A5 JP2010504181A JP2010504181A JP2010525326A5 JP 2010525326 A5 JP2010525326 A5 JP 2010525326A5 JP 2010504181 A JP2010504181 A JP 2010504181A JP 2010504181 A JP2010504181 A JP 2010504181A JP 2010525326 A5 JP2010525326 A5 JP 2010525326A5
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- Prior art keywords
- neu
- immunoassay
- cells
- cancer cells
- blood
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Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US91283307P | 2007-04-19 | 2007-04-19 | |
| PCT/US2008/060317 WO2008130910A1 (en) | 2007-04-19 | 2008-04-15 | Detection her-2/neu protein from non-isolated circulating cancer cells and treatment |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2010525326A JP2010525326A (ja) | 2010-07-22 |
| JP2010525326A5 true JP2010525326A5 (https=) | 2012-04-19 |
Family
ID=39875858
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2010504181A Pending JP2010525326A (ja) | 2007-04-19 | 2008-04-15 | 分離されていない循環癌細胞由来のＨｅｒ−２／ｎｅｕタンパク質の上昇したレベルの検出および治療 |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US20100120072A1 (https=) |
| EP (1) | EP2145188A4 (https=) |
| JP (1) | JP2010525326A (https=) |
| CN (1) | CN101663584A (https=) |
| CA (1) | CA2684265A1 (https=) |
| MX (1) | MX2009011228A (https=) |
| WO (1) | WO2008130910A1 (https=) |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ES2364495T3 (es) | 2005-02-03 | 2011-09-05 | The General Hospital Corporation | Método para tratar cáncer resistente a gefitinib. |
| JP2009514870A (ja) | 2005-11-04 | 2009-04-09 | ワイス | ｍＴＯＲインヒビター、ハーセプチン、および／またはＨＫＩ−２７２の抗悪性腫瘍性組み合わせ |
| US8022216B2 (en) | 2007-10-17 | 2011-09-20 | Wyeth Llc | Maleate salts of (E)-N-{4-[3-chloro-4-(2-pyridinylmethoxy)anilino]-3-cyano-7-ethoxy-6-quinolinyl}-4-(dimethylamino)-2-butenamide and crystalline forms thereof |
| ES2692769T3 (es) | 2008-06-17 | 2018-12-05 | Wyeth Llc | Combinaciones antineoplásicas que contienen HKI-272 y vinorelbina |
| CN105147713A (zh) | 2008-08-04 | 2015-12-16 | 惠氏有限责任公司 | 4-苯胺基-3-氰基喹啉和卡培他滨的抗肿瘤组合 |
| SG174382A1 (en) | 2009-04-06 | 2011-11-28 | Wyeth Llc | Treatment regimen utilizing neratinib for breast cancer |
| CN114805583A (zh) | 2010-05-27 | 2022-07-29 | 根马布股份公司 | 针对her2的单克隆抗体 |
| JP6082344B2 (ja) | 2010-05-27 | 2017-02-15 | ゲンマブ エー／エス | Ｈｅｒ２エピトープに対するモノクローナル抗体 |
| CA2832389A1 (en) | 2011-04-20 | 2012-10-26 | Genmab A/S | Bispecific antibodies against her2 and cd3 |
| CN104122394A (zh) * | 2013-04-23 | 2014-10-29 | 北京豪迈生物工程有限公司 | 人表皮生长因子受体2(Her-2)定量测定试剂盒及其检测方法 |
| JP6245147B2 (ja) * | 2014-11-19 | 2017-12-13 | 株式会社オートネットワーク技術研究所 | モールド部付電線 |
| CN104568923A (zh) * | 2014-12-01 | 2015-04-29 | 浙江省肿瘤医院 | 电化学发光检测外周血循环肿瘤细胞抗原的方法及试剂盒 |
| JP6323317B2 (ja) * | 2014-12-09 | 2018-05-16 | 株式会社オートネットワーク技術研究所 | 端子付電線 |
Family Cites Families (33)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6451225B1 (en) * | 1986-04-30 | 2002-09-17 | Igen International, Inc. | Electrochemiluminescent reaction utilizing amine-derived reductant |
| US5401638A (en) * | 1986-06-04 | 1995-03-28 | Oncogene Science, Inc. | Detection and quantification of neu related proteins in the biological fluids of humans |
| US4968603A (en) * | 1986-12-31 | 1990-11-06 | The Regents Of The University Of California | Determination of status in neoplastic disease |
| WO1989006692A1 (en) * | 1988-01-12 | 1989-07-27 | Genentech, Inc. | Method of treating tumor cells by inhibiting growth factor receptor function |
| US5720937A (en) * | 1988-01-12 | 1998-02-24 | Genentech, Inc. | In vivo tumor detection assay |
| US6448091B1 (en) * | 1988-11-03 | 2002-09-10 | Igen International, Inc. | Method and apparatus for improved luminescence assays using particle concentration chemiluminescence detection |
| US5801005A (en) * | 1993-03-17 | 1998-09-01 | University Of Washington | Immune reactivity to HER-2/neu protein for diagnosis of malignancies in which the HER-2/neu oncogene is associated |
| NO180658C (no) * | 1994-03-10 | 1997-05-21 | Oeystein Fodstad | Fremgangsmåte og anordning for deteksjon av spesifikke målceller i spesialiserte eller blandede cellepopulasjoner og opplösninger som inneholder blandede cellepopulasjoner |
| US5981203A (en) * | 1994-04-26 | 1999-11-09 | The Regents Of The University Of Michigan | Unitary sandwich enzyme immunoassay cassette, device and method of use |
| US5744367A (en) * | 1994-11-10 | 1998-04-28 | Igen International, Inc. | Magnetic particle based electrochemiluminescent detection apparatus and method |
| US6884357B2 (en) * | 1995-02-21 | 2005-04-26 | Iqbal Waheed Siddiqi | Apparatus and method for processing magnetic particles |
| US5783404A (en) * | 1995-04-13 | 1998-07-21 | Amgen Inc. | Methods and compositions for determining HER-2/neu expression using monoclonal antibodies |
| DE69637001T2 (de) * | 1995-06-07 | 2007-12-06 | Bioveris Corp. | Elektrochemilumineszenz-enzymimmunoassay |
| US6117985A (en) * | 1995-06-16 | 2000-09-12 | Stemcell Technologies Inc. | Antibody compositions for preparing enriched cell preparations |
| US6190870B1 (en) * | 1995-08-28 | 2001-02-20 | Amcell Corporation | Efficient enrichment and detection of disseminated tumor cells |
| US6297062B1 (en) * | 1996-03-07 | 2001-10-02 | Bio-Magnetics Ltd. | Separation by magnetic particles |
| US6890426B2 (en) * | 1996-06-07 | 2005-05-10 | Immunivest Corporation | Magnetic separation apparatus and methods |
| US20020172987A1 (en) * | 1998-02-12 | 2002-11-21 | Terstappen Leon W.M.M. | Methods and reagents for the rapid and efficient isolation of circulating cancer cells |
| WO1999041613A1 (en) * | 1998-02-12 | 1999-08-19 | Immunivest | Methods and reagents for the rapid and efficient isolation of circulating cancer cells |
| AU2876900A (en) * | 1999-02-10 | 2000-08-29 | Cell Works Inc. | Class characterization of circulating cancer cells isolated from body fluids andmethods of use |
| US6300143B1 (en) * | 1999-03-01 | 2001-10-09 | Idec Pharmaceuticals Corporation | Electrochemiluminescent assays for eukaryotic cells |
| US6969615B2 (en) * | 1999-07-26 | 2005-11-29 | 20/20 Genesystems, Inc. | Methods, devices, arrays and kits for detecting and analyzing biomolecules |
| US7537938B2 (en) * | 2000-04-28 | 2009-05-26 | Monogram Biosciences, Inc. | Biomarker detection in circulating cells |
| JP3313107B2 (ja) * | 2001-03-22 | 2002-08-12 | バイエル コーポレイション | ヒトの生物学的流体中のｎｅｕ関連タンパク質の検出及び定量 |
| DE10143776A1 (de) * | 2001-09-06 | 2003-04-03 | Adnagen Ag | Verfahren und Kit zur Diagnostik oder Behandlungskontrolle von Brustkrebs |
| DE60237531D1 (de) * | 2001-10-11 | 2010-10-14 | Aviva Biosciences Corp | Verfahren zum trennen von seltenen zellen von fluidproben |
| EP1597353B1 (en) * | 2003-02-27 | 2010-11-24 | Veridex, LLC | CIRCULATING TUMOR CELLS (CTC's): EARLY ASSESSMENT OF TIME TO PROGRESSION SURVIVAL AND RESPONSE TO THERAPY IN METASTATIC CANCER PATIENTS |
| CA2582713A1 (en) * | 2004-10-06 | 2006-04-20 | Wellstat Biologics Corporation | Detection of elevated levels of her-2/neu protein on circulating cancer cells and treatment |
| GB0512429D0 (en) * | 2005-06-17 | 2005-07-27 | Smithkline Beecham Corp | Novel compound |
| EP1816477A1 (en) * | 2006-02-06 | 2007-08-08 | F. Hoffmann-la Roche AG | The use of natriuretic peptides and placenta growth factor levels for risk stratification of individuals elected for cardiac stress testing |
| MX2008013331A (es) * | 2006-04-18 | 2008-11-10 | Wellstat Biologics Corp | Deteccion de receptores de esteroides en celulas de carcinoma circulantes y tratamiento. |
| EP2008102A4 (en) * | 2006-04-18 | 2009-07-08 | Wellstat Biologics Corp | DETECTION OF PROTEINS IN NEOPLASTIC CELLS IN CIRCULATION |
| US8557531B2 (en) * | 2006-04-18 | 2013-10-15 | Wellstat Biologics Corporation | Detection of circulating endothelial cells |
-
2008
- 2008-04-15 CA CA002684265A patent/CA2684265A1/en not_active Abandoned
- 2008-04-15 WO PCT/US2008/060317 patent/WO2008130910A1/en not_active Ceased
- 2008-04-15 MX MX2009011228A patent/MX2009011228A/es active IP Right Grant
- 2008-04-15 US US12/593,160 patent/US20100120072A1/en not_active Abandoned
- 2008-04-15 JP JP2010504181A patent/JP2010525326A/ja active Pending
- 2008-04-15 CN CN200880012580A patent/CN101663584A/zh active Pending
- 2008-04-15 EP EP08745839A patent/EP2145188A4/en not_active Withdrawn
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